Canonical Allele Identifier: PA2825515399
Gene: WHRN HGNC NCBI

Linked Data

ClinVar Variation Id: 199137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001077354.2:p.Val352Ile
CA248169
NM_001083885.3:c.1054G>A